Genetics & Preventive Genomics
On this page
Get care
Why choose UCSF Health for genetics and preventive genomics services?
UCSF Health offers one of the few comprehensive genetic and preventive genomics programs in the U.S.
Many health conditions run in families, passed from parent to child. Our team helps you understand your inherited risk and what you can do to lower it or catch disease early. We evaluate genetic forms of many conditions, such as cancer, heart disease, dementia and diabetes.
As one of the few programs using preventive genomics, we're at the forefront of preventing and treating inherited diseases. Preventive genomics analyzes all your genetic information to guide personalized health strategies.
Why choose UCSF Health for genetics and preventive genomics services?
UCSF Health offers one of the few comprehensive genetic and preventive genomics programs in the U.S.
Many health conditions run in families, passed from parent to child. Our team helps you understand your inherited risk and what you can do to lower it or catch disease early. We evaluate genetic forms of many conditions, such as cancer, heart disease, dementia and diabetes.
As one of the few programs using preventive genomics, we're at the forefront of preventing and treating inherited diseases. Preventive genomics analyzes all your genetic information to guide personalized health strategies.
Get care
Leading the way in pharmacogenomics
We're one of the few U.S. health systems offering hospital-wide pharmacogenomic testing to help tailor medications and doses to your genetics.Whole genome sequencing
Our advanced sequencing technology enables us to analyze your entire genome, providing a comprehensive understanding of your genetic risks and conditions.Rare disease evaluation
Using innovative techniques, we help diagnose unexplained or rare conditions for people who have not found answers elsewhere.Family-wide genetic support
If we identify a genetic condition or risk, we can help your relatives access testing, monitoring and ongoing care.
Multi-specialty genetics and preventive genomics expertise at UCSF Health
Our team works together to screen patients for genetic conditions, including people with a family history of disease that suggests a hereditary component. By understanding your genetic risks, we can work with you to prevent disease, choose the most effective treatments and make informed decisions.
Our understanding of genes and variants is always evolving. To keep your results current, we can re-analyze prior genome sequencing when initial findings are inconclusive or when your health or family history changes. Re-analysis ensures you have the most up-to-date information to guide your care.
Medical genetics specialists and genetic counselors collaborate closely with experts in other specialties, including:
Cardiology for genetic heart conditions
Neurology for neurodegenerative disorders and epilepsy
Oncology for cancer care and surveillance
Pharmacology and pharmacy for medication management
You have access to any other UCSF Health specialty as needed, depending on your diagnosis or risk factors. This approach ensures you benefit from the expertise of our broad network of specialists and receive coordinated, personalized care.
Family planning
Advanced genetic testing services can help people planning a pregnancy. We offer carrier screening and genetic counseling to help you assess and understand your risk of passing genetic conditions to your children.
Our experts also offer guidance on reproductive options to prevent transmission of genetic diseases, such as pre-implantation genetic testing. By identifying genetic risks before or during family planning, you can make informed decisions about the health of your future children.
Unique pharmacogenomics expertise
Pharmacogenomics studies how your genetic makeup affects your response to medications.
UCSF Health is one of the only hospitals nationwide offering pharmacogenomic testing to help determine which medications are most effective and safest for you. Understanding your unique genetics reduces the risk of serious drug reactions and helps us personalize your treatment.
NF/Ras pathway
Ras pathway disorders, such as neurofibromatosis (NF), are genetic conditions that can cause several health issues, including heart defects and problems with muscles, bones and skin. Our NF/Ras experts provide care, support and management for people who have or are at risk for one of these disorders.
We offer referral services to a network of more than 50 UCSF Health specialists with expertise in Ras pathway disorders. All of your affected family members receive comprehensive, coordinated care, with a seamless transition from pediatric to adult care specialists. Genetic counselors provide education and supportive resources for you and your family. We can also connect you with clinical trials for next-generation treatments for Ras pathway disorders.
Providers
Kanika Bhardwaj, MD
Medical Genetics
Randeep Kaur Brar, MD
Medical Genetics
Soghra Jougheh Doust, MD
Clinical Genetics
Aleksandar Rajkovic, MD, PhD
Medical Genetics • Obstetrics and Gynecology
Explore what we do
FAQ: Genetic Testing for Hereditary Cancer
If you have a family history of cancer, a genetic counselor can help you understand your cancer risk. Read FAQs about genetic testing for hereditary cancer.
Award-winning care
Best in the West and No. 2 in the nation for neurology & neurosurgery
One of the nation's best for heart & vascular care
Best in California and No. 7 in the nation for cancer care
Related conditions & treatments
Conditions
- Genetic Disorders
- Neurofibromatosis